Department of Urology & Uro-Oncology, Hannover Medical School, Hannover 30625, Germany.
J Sex Med. 2009 Oct;6(10):2672-9. doi: 10.1111/j.1743-6109.2009.01423.x. Epub 2009 Aug 4.
It has been suggested that serotonin re-uptake inhibitors (SRIs) may retard the ejaculatory response by acting directly on the seminal vesicle (SV) and ductus deferens smooth muscle. However, until now, only a very few experimental studies have investigated such potential local (peripheral) effects.
To elucidate the effects of serotonin (5-HT) and the SRIs clomipramine, fluoxetine and imipramine on the tension induced by norepinephrine (NE) of isolated human SV smooth muscle, as well as on the production of tissue cyclic AMP and cyclic GMP.
To measure the inhibition exerted by serotonin and SRIs clomipramine, fluoxetine, and imipramine on the contractile response of isolated SV tissue. In addition, the effects of the drugs on the turn-over of cyclic nucleotides cAMP and cGMP were also elucidated.
The effects of the cumulative addition of serotonin and the SRIs clomipramine, fluoxetine and imipramine (1 nM-10 microM) on the tension induced by the alpha(1)-adrenoceptor agonist NE (10 microM) of SV strip preparations were studied using the organ bath technique. Cyclic AMP and cyclic GMP were measured by means of specific radioimmunoassays.
The tension induced by NE was dose-dependently reversed by the drugs tested. The rank order of efficacy was: imipramine > or = fluoxetine > or = clomipramine > serotonin. Mean reversion of tension was measured between 66 +/- 6.6% and 52 +/- 6.6%. These effects were paralleled by a 1.3-fold to 2.7-fold increase in tissue cAMP in response to exposure to the drugs. In contrast, no significant enhancement in cGMP was noted.
The findings, for the first time, present evidence that SRIs may antagonize the sympathetic contraction of SV smooth muscle via stimulation of tissue cyclic AMP.
有人提出,5-羟色胺再摄取抑制剂(SSRIs)可能通过直接作用于精囊(SV)和输精管平滑肌来延缓射精反应。然而,到目前为止,只有极少数的实验研究调查了这种潜在的局部(外周)效应。
阐明 5-羟色胺(5-HT)和 SSRIs 氯米帕明、氟西汀和丙咪嗪对分离的人 SV 平滑肌对去甲肾上腺素(NE)诱导的张力的影响,以及对组织环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)产生的影响。
测量 5-HT 和 SSRIs 氯米帕明、氟西汀和丙咪嗪对 SV 组织收缩反应的抑制作用。此外,还阐明了药物对环核苷酸 cAMP 和 cGMP 周转率的影响。
使用器官浴技术研究了 5-HT 和 SSRIs 氯米帕明、氟西汀和丙咪嗪(1 nM-10 μM)的累积添加对 SV 带制剂中 α1-肾上腺素受体激动剂 NE(10 μM)诱导的张力的影响。通过特异性放射免疫测定法测量 cAMP 和 cGMP。
NE 诱导的张力被测试药物剂量依赖性地逆转。药物的疗效顺序为:丙咪嗪>或=氟西汀>或=氯米帕明>5-HT。张力的平均恢复程度在 66+/-6.6%和 52+/-6.6%之间。这些效应与暴露于药物时组织 cAMP 增加 1.3 到 2.7 倍相平行。相比之下,没有观察到 cGMP 的显著增强。
这些发现首次提供了证据,表明 SSRIs 可能通过刺激组织 cAMP 拮抗 SV 平滑肌的交感收缩。